2(1H)-Pyridinone, 5-benzoyl-6-(ethylthio)-1-methyl-

Base Information

Chemical Name:2(1H)-Pyridinone, 5-benzoyl-6-(ethylthio)-1-methyl-
CAS No.:602309-16-0
Molecular Formula:C15H15NO2S
Molecular Weight:273.35000
Hs Code.:

Synonyms:5-benzoyl-6-(ethylsulfanyl)-1-methyl-2(1H)-pyridinone;2(1H)-Pyridinone,5-benzoyl-6-(ethylthio)-1-methyl;

Suppliers and Price of 2(1H)-Pyridinone, 5-benzoyl-6-(ethylthio)-1-methyl-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2(1H)-Pyridinone, 5-benzoyl-6-(ethylthio)-1-methyl-

Chemical Property:

PSA：64.37000
LogP:2.72830

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2(1H)-Pyridinone, 5-benzoyl-6-(ethylthio)-1-methyl-

There total 4 articles about 2(1H)-Pyridinone, 5-benzoyl-6-(ethylthio)-1-methyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 45.0%

: 73843-97-7
3-(ethylthio)-3-(methylamino)-1-phenylprop-2-en-1-one

: 922-67-8
propynoic acid methyl ester

: 602309-16-0
5-benzoyl-6-(ethylsulfanyl)-1-methyl-2(1H)-pyridinone

Guidance literature:: DOI:10.1055/s-2005-872217

Reference yield: 40.0%

: 3-(ethylsulfanyl)-3-(methylamino)-1-phenyl-2-propen-1-one

: 922-67-8
propynoic acid methyl ester

: 602309-16-0
5-benzoyl-6-(ethylsulfanyl)-1-methyl-2(1H)-pyridinone

Guidance literature:: In methanol; for 20h; Heating / reflux;

Reference yield:

: 56617-74-4
N-methyl-3-oxo-3-phenyl-propanethioamide

: 602309-16-0
5-benzoyl-6-(ethylsulfanyl)-1-methyl-2(1H)-pyridinone

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / 2 h / 20 °C

With potassium carbonate; In acetone;
DOI:10.1055/s-2005-872217